UDI system (Saudi- DI) aims to record and document the identifier codes for medical devices based on international standards. Device (DI) codes will help the users and stakeholders to recognize all information related to the device through registered UDI codes and labeled on the device package

National Center for Medical Devices Reporting ( NCMDR ) A systematic database to manage medical devices' post-market activities, such as Medical devices reporting of Adverse events and complaints, as well as publishing the Safety alerts of Medical devices with follow-up implementation of the corrective actions to ensure the safety, efficacy and performance of medical devices.

electronic system through which requests for approval of technical and clinical specifications for medical radioactive materials for the benefit of medical establishment are received which requested by importer, re-exporter and transporter establishments of these materials, and then approval of technical and clinical specifications is issued, before applying for importing or re-exporting clearance